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地西他滨治疗难治性贫血伴有原始细胞过多的疗效和不良反应与治疗疗程数的关系
OBJECTIVE: To explore the impact of decitabine treatment cycles on efficacy and adverse events (AEs) in patients of myelodysplastic syndrome-refractory anemia with excess blasts (MDSRAEB). METHODS: A total of fifty-six patients with MDS-RAEB who received decitabine 20 mg·m(−2)·d(−1)by IV infusion da...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
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Editorial office of Chinese Journal of Hematology
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364885/ https://www.ncbi.nlm.nih.gov/pubmed/27801319 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2016.10.011 |
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collection | PubMed |
description | OBJECTIVE: To explore the impact of decitabine treatment cycles on efficacy and adverse events (AEs) in patients of myelodysplastic syndrome-refractory anemia with excess blasts (MDSRAEB). METHODS: A total of fifty-six patients with MDS-RAEB who received decitabine 20 mg·m(−2)·d(−1)by IV infusion daily for 5 consecutive days every 4 weeks at a single institute in China were enrolled from December 2008 to March 2016. Their clinical features, efficacy, predictors of efficacy and AEs were analyzed retrospectively. RESULTS: Of the 56 patients enrolled, 25 cases were MDS-RAEB1, another 31 were MDS-RAEB2. A median of 3 cycles (range, 1–15 cycles) were delivered. The overall response rate was 67.9% (10 complete responses, 8 marrow complete responses without hematologic improvement, 17 marrow complete responses with hematologic improvements, and 3 hematologic improvements). With a median follow-up duration of 7.9(1.0–56.3) months, the median overall survival was 21.1(95% CI 16.0–26.1) months. Compared with RAEB-2, RAEB-1 predicted higher overall response rates in a multivariate analysis. Of the 38 patients who experienced clinical responses, initial responses were detected by the end of two cycles in 37 patients. Twenty-five of the 38 patients who experienced clinical responses had their best response within the first two cycles, and 37 cases of the patients achieved best response by the end of fourth cycles. Grade 3 or 4 cytopenia and infection were the most prevalent AEs, which occurred frequently in the early courses and decreased later, and other non-hematologic AEs were rare. CONCLUSION: Decitabine treatment was favorable in patients with MDS-RAEB. In most of the cases, initial responses were observed within 2 cycles, and best response was achieved by the end of 4 th cycles. The most common AEs were grade 3 or 4 cytopenia and infection, which were observed frequently in first 2 cycles and decreased later as objective response were achieved. |
format | Online Article Text |
id | pubmed-7364885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Editorial office of Chinese Journal of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73648852020-07-16 地西他滨治疗难治性贫血伴有原始细胞过多的疗效和不良反应与治疗疗程数的关系 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To explore the impact of decitabine treatment cycles on efficacy and adverse events (AEs) in patients of myelodysplastic syndrome-refractory anemia with excess blasts (MDSRAEB). METHODS: A total of fifty-six patients with MDS-RAEB who received decitabine 20 mg·m(−2)·d(−1)by IV infusion daily for 5 consecutive days every 4 weeks at a single institute in China were enrolled from December 2008 to March 2016. Their clinical features, efficacy, predictors of efficacy and AEs were analyzed retrospectively. RESULTS: Of the 56 patients enrolled, 25 cases were MDS-RAEB1, another 31 were MDS-RAEB2. A median of 3 cycles (range, 1–15 cycles) were delivered. The overall response rate was 67.9% (10 complete responses, 8 marrow complete responses without hematologic improvement, 17 marrow complete responses with hematologic improvements, and 3 hematologic improvements). With a median follow-up duration of 7.9(1.0–56.3) months, the median overall survival was 21.1(95% CI 16.0–26.1) months. Compared with RAEB-2, RAEB-1 predicted higher overall response rates in a multivariate analysis. Of the 38 patients who experienced clinical responses, initial responses were detected by the end of two cycles in 37 patients. Twenty-five of the 38 patients who experienced clinical responses had their best response within the first two cycles, and 37 cases of the patients achieved best response by the end of fourth cycles. Grade 3 or 4 cytopenia and infection were the most prevalent AEs, which occurred frequently in the early courses and decreased later, and other non-hematologic AEs were rare. CONCLUSION: Decitabine treatment was favorable in patients with MDS-RAEB. In most of the cases, initial responses were observed within 2 cycles, and best response was achieved by the end of 4 th cycles. The most common AEs were grade 3 or 4 cytopenia and infection, which were observed frequently in first 2 cycles and decreased later as objective response were achieved. Editorial office of Chinese Journal of Hematology 2016-10 /pmc/articles/PMC7364885/ /pubmed/27801319 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2016.10.011 Text en 2016年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal. |
spellingShingle | 论著 地西他滨治疗难治性贫血伴有原始细胞过多的疗效和不良反应与治疗疗程数的关系 |
title | 地西他滨治疗难治性贫血伴有原始细胞过多的疗效和不良反应与治疗疗程数的关系 |
title_full | 地西他滨治疗难治性贫血伴有原始细胞过多的疗效和不良反应与治疗疗程数的关系 |
title_fullStr | 地西他滨治疗难治性贫血伴有原始细胞过多的疗效和不良反应与治疗疗程数的关系 |
title_full_unstemmed | 地西他滨治疗难治性贫血伴有原始细胞过多的疗效和不良反应与治疗疗程数的关系 |
title_short | 地西他滨治疗难治性贫血伴有原始细胞过多的疗效和不良反应与治疗疗程数的关系 |
title_sort | 地西他滨治疗难治性贫血伴有原始细胞过多的疗效和不良反应与治疗疗程数的关系 |
topic | 论著 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364885/ https://www.ncbi.nlm.nih.gov/pubmed/27801319 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2016.10.011 |
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